EP2723490A2 - Hydrogen sulfide scavenger for use in hydrocarbons - Google Patents
Hydrogen sulfide scavenger for use in hydrocarbonsInfo
- Publication number
- EP2723490A2 EP2723490A2 EP12802517.8A EP12802517A EP2723490A2 EP 2723490 A2 EP2723490 A2 EP 2723490A2 EP 12802517 A EP12802517 A EP 12802517A EP 2723490 A2 EP2723490 A2 EP 2723490A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- hydrogen sulfide
- sulfide scavenger
- polyamine
- hydrocarbon
- glycol mono
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 title claims abstract description 69
- 229910000037 hydrogen sulfide Inorganic materials 0.000 title claims abstract description 69
- 239000002516 radical scavenger Substances 0.000 title claims abstract description 50
- 229930195733 hydrocarbon Natural products 0.000 title claims description 34
- 150000002430 hydrocarbons Chemical class 0.000 title claims description 34
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 claims abstract description 40
- 229940015043 glyoxal Drugs 0.000 claims abstract description 20
- 238000007670 refining Methods 0.000 claims abstract description 12
- 239000010779 crude oil Substances 0.000 claims abstract description 5
- 229920000768 polyamine Polymers 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 24
- 239000004215 Carbon black (E152) Substances 0.000 claims description 19
- 239000002270 dispersing agent Substances 0.000 claims description 13
- 239000007795 chemical reaction product Substances 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 7
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 6
- UPGSWASWQBLSKZ-UHFFFAOYSA-N 2-hexoxyethanol Chemical compound CCCCCCOCCO UPGSWASWQBLSKZ-UHFFFAOYSA-N 0.000 claims description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 5
- -1 Methylene tetramine Chemical compound 0.000 claims description 5
- 239000010426 asphalt Substances 0.000 claims description 5
- XYVAYAJYLWYJJN-UHFFFAOYSA-N 2-(2-propoxypropoxy)propan-1-ol Chemical compound CCCOC(C)COC(C)CO XYVAYAJYLWYJJN-UHFFFAOYSA-N 0.000 claims description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 150000001735 carboxylic acids Chemical class 0.000 claims description 4
- 239000000047 product Substances 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 4
- 239000003129 oil well Substances 0.000 claims description 3
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 claims description 2
- WMDZKDKPYCNCDZ-UHFFFAOYSA-N 2-(2-butoxypropoxy)propan-1-ol Chemical compound CCCCOC(C)COC(C)CO WMDZKDKPYCNCDZ-UHFFFAOYSA-N 0.000 claims description 2
- GZMAAYIALGURDQ-UHFFFAOYSA-N 2-(2-hexoxyethoxy)ethanol Chemical compound CCCCCCOCCOCCO GZMAAYIALGURDQ-UHFFFAOYSA-N 0.000 claims description 2
- JDSQBDGCMUXRBM-UHFFFAOYSA-N 2-[2-(2-butoxypropoxy)propoxy]propan-1-ol Chemical compound CCCCOC(C)COC(C)COC(C)CO JDSQBDGCMUXRBM-UHFFFAOYSA-N 0.000 claims description 2
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical class CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 claims description 2
- WGKZYJXRTIPTCV-UHFFFAOYSA-N 2-butoxypropan-1-ol Chemical compound CCCCOC(C)CO WGKZYJXRTIPTCV-UHFFFAOYSA-N 0.000 claims description 2
- PSKIVCBTSGNKBB-UHFFFAOYSA-N 2-propoxypropan-1-ol Chemical compound CCCOC(C)CO PSKIVCBTSGNKBB-UHFFFAOYSA-N 0.000 claims description 2
- MFKRHJVUCZRDTF-UHFFFAOYSA-N 3-methoxy-3-methylbutan-1-ol Chemical compound COC(C)(C)CCO MFKRHJVUCZRDTF-UHFFFAOYSA-N 0.000 claims description 2
- 239000001273 butane Substances 0.000 claims description 2
- YMHQVDAATAEZLO-UHFFFAOYSA-N cyclohexane-1,1-diamine Chemical compound NC1(N)CCCCC1 YMHQVDAATAEZLO-UHFFFAOYSA-N 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 2
- 229920000847 nonoxynol Polymers 0.000 claims description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims description 2
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 abstract description 5
- 238000005260 corrosion Methods 0.000 abstract description 4
- 230000007797 corrosion Effects 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 2
- 239000003345 natural gas Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 abstract 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 abstract 1
- 239000000463 material Substances 0.000 description 7
- 239000000446 fuel Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000002000 scavenging effect Effects 0.000 description 2
- 150000003335 secondary amines Chemical group 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000609499 Palicourea Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000011143 downstream manufacturing Methods 0.000 description 1
- 235000011167 hydrochloric acid Nutrition 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000005504 petroleum refining Methods 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/04—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
- C08G12/06—Amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/20—Organic compounds not containing metal atoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2208/00—Aspects relating to compositions of drilling or well treatment fluids
- C09K2208/20—Hydrogen sulfide elimination
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1025—Natural gas
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1033—Oil well production fluids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/201—Impurities
- C10G2300/207—Acid gases, e.g. H2S, COS, SO2, HCN
Definitions
- the invention relates to additives useful for reducing the concentration of hydrogen sulfide in hydrocarbons.
- the invention particularly relates to additives that are a system of components and their use in hydrocarbons to scavenge hydrogen sulfide.
- Hydrocarbons such as crude oil, may contain acids in several forms. These acids may be mineral acids such as hydrochloric and phosphoric acids. A common inorganic acid found in hydrocarbons is hydrogen sulfide and various oxidized forms of hydrogen sulfide such as sulfuric acid.
- Hydrogen sulfide is both toxic and corrosive. Neither of these properties is usually desirable in hydrocarbons.
- Hydrogen sulfide may be present when crude oil is produced from an oil well. It may also be present or created by decomposition of other sulfur containing compounds during a refining process. If not removed, generally by scavenging, it may still be present after refining in hydrocarbon products ranging from light lubricating oils to fuels to heavy fuels to bitumen. It would therefor be desirable in the art of producing and refining hydrocarbons to reduce or remove hydrogen sulfide from the hydrocarbons.
- the invention may be a hydrogen sulfide scavenger including a reaction product of glyoxal and a polyamine.
- the hydrogen sulfide scavenger may also include a dispersant.
- the invention may be the product of treating a hydrocarbon with a hydrogen sulfide scavenger wherein the hydrogen sulfide scavenger includes a reaction product of glyoxal and a polyamine.
- the invention may be a method of treating a hydrocarbon with a hydrogen sulfide scavenger wherein the hydrogen sulfide scavenger includes a reaction product of glyoxal and a polyamine.
- the method may also include using a dispersant as a component of the hydrogen sulfide scavenger.
- a hydrogen sulfide scavenger may be a system of components including the reaction product of glyoxal and a polyamine.
- Glyoxal has the structure:
- polyamine shall mean a compound having 2 or more primary or secondary amine groups or at least one primary and one secondary amine group. These compounds shall include at least 2 carbons and may have as many as 12 carbons. In some embodiments, the polyamine may have from about 2 to about 10 carbons. In still other embodiments, the polyamine may have from about 2 to about 6 carbons.
- the polyamines may be linear, branched, or cycloaliphatic.
- Exemplary polyamines useful with the method of the disclosure include ethylene diamine (EDA), diethylene triamine (DETA), Methylene tetramine (TETA), tetraethylene pentamine (TEPA), piperazine, cyclohexane diamine, butane diamine, and combinations thereof.
- EDA ethylene diamine
- DETA diethylene triamine
- TETA Methylene tetramine
- TEPA tetraethylene pentamine
- piperazine cyclohexane diamine
- butane diamine and combinations thereof.
- a reaction product of glyoxal and a polyamine is employed as a component of a hydrogen sulfide scavenger.
- the subject reaction product is a product prepared by a process including introducing the glyoxal with the polyamine under reaction conditions to induce an exothermic reaction. Any method known to be useful to those of ordinary skill in
- the equivalent ratio of glyoxal to polyamine in some embodiments of the method of the disclosure, may be from about 1 :9 to about 9:1. In other embodiments the equivalent ratio of the glyoxal to the polyamine may be from about 1:7 to about 7:1. In still other embodiments, the equivalent ratio of the glyoxal to the polyamine may be from about 1:4 to about 2: 1. In yet other embodiments, the equivalent ratio of the glyoxal to the polyamine may be about 1:1.
- the reaction product may not be as compatible as desired in a hydrocarbon being treated and thus a dispersant may be employed.
- the dispersant used may be cationic, anionic or non- ionic.
- Exemplary dispersants include, but are not limited to mono-ethylene glycol n- hexyl ether (Hexyl Cellosolve[R] available from Union Carbide); ethylene glycol monobutyl ether (Butyl Cellosolve[R]); di- and tri-propylene glycol derivatives of propyl and butyl alcohol, which are available from Arco Chemical (3801 West Chester Pike, Newtown Square, Pa. 19073) and Dow Chemical (1691 N.
- Polymeric dispersants may also be used.
- ethoxylated long chain and/or branched alcohols, ethoxylated carboxylic acids, and ethoxylated nonylphenols having from about 2 to about 11 ethylene oxide (EO) units ethoxylated long chain and branched alcohols, ethoxylated carboxylic acids, and ethoxylated esters of glycerol may be useful with some embodiments of the methods of the disclosure.
- EO ethylene oxide
- the hydrogen sulfide scavenger system may consist essentially of only the glyoxal and polyamine reaction product.
- the terms "consisting essentially of means that the hydrogen sulfide scavenger has no more than 5 percent by weight or, in some embodiments, no more than 1 percent by weight of any other nitrogen containing components.
- the hydrogen sulfide scavenger is prepared without a dispersant.
- the hydrogens sulfide scavenger claimed herein are useful in treating hydrocarbons.
- the hydrocarbons may be crude, partially refined, or fully refined and pending commercial consumption.
- the hydrocarbons to be treated are crude hydrocarbons, in one embodiment they may be very "crude” and be, for example, crude oil.
- the crude hydrocarbon may only be "crude” in regard to a subsequent refining step.
- the method of the disclosure may be a refining step to produce light hydrocarbon fuels such as gasoline or aviation fuel.
- the feed streams for such units have already undergone at least one step to remove components that are not desirable for producing such fuels.
- the feed stream to this unit is a crude hydrocarbon even though it has had at least one refining process step already performed upon it.
- the hydrocarbon being treated with a hydrogen sulfide scavenger is asphalt.
- asphalt refers to any of a variety of materials that are solid or semisolid at room temperature and which gradually liquefy when heated, and in which the predominant constituents are naturally occurring bitumens (or kerogens) or which are bitumen like materials obtained as residue in petroleum refining.
- the total feed rate of the hydrogen sulfide scavenger will generally be determined by the operator of the specific production process unit to be subjected to treatment using the claimed hydrogen sulfide scavengers. Those of ordinary skill in the art in operating such a unit will know how to make such determinations based upon the specific operating parameters of their production units. Nevertheless, in some embodiments, the feed rate of the hydrogen sulfide scavengers will be from about 10 to 10,000 ppm in the process stream being treated. In other embodiments, the feed rate will be from about 100 to 1,000 ppm. In still other embodiments, the feed range will be from about 200 to about 800 ppm.
- this rate is based upon a ratio of the scavenger to the hydrogens sulfide present. Such ratios are often based upon weight and can range, in some embodiments of the method of the disclosure, from (scavenger: hydrogen sulfide) about 1 :200 to about 200: 1.
- the hydrogen sulfide scavengers of the application may be introduced into their target feed material in any way known to be useful to those of ordinary skill in the art subject to the caveat that the hydrogen sulfide scavengers are introduced prior to or concurrent with the a refining process.
- the hydrogen sulfide scavenger is injected into the feed material upstream from a refining unit as the feed material passes through a turbulent section of piping.
- the hydrogen sulfide scavenger is admixed with the feed material in a holding vessel that is agitated.
- the hydrogen sulfide scavenger is admixed with the feed immediately upstream of a refining unit by injecting the hydrogen sulfide scavenger into a turbulent flow, the turbulent flow being created by static mixers put into place for the purpose of admixing the hydrogen sulfide scavenger with a feed material.
- the hydrogen sulfide scavenger is atomized and fed into a vaporous feed stream using, for example, an injection quill.
- the hydrogen sulfide scavengers may be introduced in any way useful for the target application.
- the scavenger may be introduced downhole or into the above ground equipment as are other, conventional scavengers.
- the claimed scavengers may also be introduced into pipelines, storage vessels and even into mobile storage vessels such as trucks, rail cars, and ship holds. Is some embodiments, scavengers are actively mixed and in others passively mixed with the hydrocarbons being treated.
- Condensate a liquid under ambient conditions which is a mixture of low molecular weight alkanes, is sparged with nitrogen having a hydrogen sulfide concentration of 1 % for 1 hour.
- the concentration of the hydrogen sulfide in the condensate prior to treatment is determined to be 19.9 ppm.
- the condensate is then tested by introducing a hydrogen sulfide scavenger prepared by reacting glyoxal and DETA at a molar ratio of 1:1 (which is an equivalent ratio of 1 :2).
- the treated condensate and a blank were shaken using an orbital shaker at 400 rpm at ambient conditions for 4 hours.
- the blank was retested and had a hydrogens sulfide concentration of 10.5 ppm.
- the treated sample showed no measurable hydrogen sulfide ( ⁇ 0.5 ppm).
- Example 1 was repeated substantially identically except that the initial concentration of hydrogen sulfide was 30.8 ppm and the hydrogen sulfide scavenger was introduced at a concentration of 300 ppm. After treatment, the blank has a hydrogen sulfide concentration of 13.1 ppm. The treated sample showed no measurable hydrogen sulfide ( ⁇ 0.5 ppm).
- Example 3
- the hydrogen scavenger of Example 1 is used to immerse carbon steel corrosion coupons.
- the immersed coupons were held at about 40°C for 14 days.
- the corrosion rate was determined to be about 19.19 mpy.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Gas Separation By Absorption (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL12802517T PL2723490T3 (en) | 2011-06-21 | 2012-06-20 | Hydrogen sulfide scavenger for use in hydrocarbons |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161499513P | 2011-06-21 | 2011-06-21 | |
US13/527,105 US9394396B2 (en) | 2011-06-21 | 2012-06-19 | Hydrogen sulfide scavenger for use in hydrocarbons |
PCT/US2012/043361 WO2012177771A2 (en) | 2011-06-21 | 2012-06-20 | Hydrogen sulfide scavenger for use in hydrocarbons |
Publications (3)
Publication Number | Publication Date |
---|---|
EP2723490A2 true EP2723490A2 (en) | 2014-04-30 |
EP2723490A4 EP2723490A4 (en) | 2015-01-28 |
EP2723490B1 EP2723490B1 (en) | 2020-07-29 |
Family
ID=47362440
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP12802517.8A Active EP2723490B1 (en) | 2011-06-21 | 2012-06-20 | Hydrogen sulfide scavenger for use in hydrocarbons |
Country Status (8)
Country | Link |
---|---|
US (1) | US9394396B2 (en) |
EP (1) | EP2723490B1 (en) |
CN (1) | CN103619466A (en) |
CA (1) | CA2839138C (en) |
ES (1) | ES2823824T3 (en) |
HU (1) | HUE051751T2 (en) |
PL (1) | PL2723490T3 (en) |
WO (1) | WO2012177771A2 (en) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120012507A1 (en) * | 2010-07-14 | 2012-01-19 | Compton Dennis R | Use of alpha-amino ethers for the removal of hydrogen sulfide from hydrocarbons |
US20120012505A1 (en) * | 2010-07-14 | 2012-01-19 | Compton Dennis R | Use of alpha-amino ethers for the removal of mercaptans from hydrocarbons |
ITRM20130245A1 (en) * | 2013-04-24 | 2014-10-25 | Chimec Spa | NEW SCAVENGERS OF SULFIDRIC ACID |
US9663390B2 (en) | 2013-05-10 | 2017-05-30 | Ecolab Usa Inc. | Reduction of hydrogen sulfide and/or malodor gassing from water via the addition of peroxyacetic acid/hydrogen peroxide product |
CN103468229B (en) * | 2013-09-24 | 2015-07-22 | 克拉玛依市义恩技术服务有限责任公司 | Solid-free and high-viscosity separation agent for well completion fluid |
DE102015121689A1 (en) * | 2015-12-14 | 2017-06-14 | Schülke & Mayr GmbH | Use of compositions containing 3,3'-methylenebis (5-methyloxazolidine) in the removal of sulfur compounds from process streams |
CN108430603B (en) * | 2016-01-05 | 2021-05-25 | 多尔夫凯塔尔化学制品(I)私人有限公司 | Additive composition for scavenging hydrogen sulfide and method of use thereof |
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- 2012-06-19 US US13/527,105 patent/US9394396B2/en not_active Expired - Fee Related
- 2012-06-20 EP EP12802517.8A patent/EP2723490B1/en active Active
- 2012-06-20 HU HUE12802517A patent/HUE051751T2/en unknown
- 2012-06-20 WO PCT/US2012/043361 patent/WO2012177771A2/en unknown
- 2012-06-20 CN CN201280030338.0A patent/CN103619466A/en active Pending
- 2012-06-20 PL PL12802517T patent/PL2723490T3/en unknown
- 2012-06-20 CA CA2839138A patent/CA2839138C/en not_active Expired - Fee Related
- 2012-06-20 ES ES12802517T patent/ES2823824T3/en active Active
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Also Published As
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WO2012177771A2 (en) | 2012-12-27 |
CA2839138C (en) | 2018-05-01 |
WO2012177771A3 (en) | 2013-04-11 |
EP2723490B1 (en) | 2020-07-29 |
CA2839138A1 (en) | 2012-12-27 |
HUE051751T2 (en) | 2021-03-29 |
ES2823824T3 (en) | 2021-05-10 |
US9394396B2 (en) | 2016-07-19 |
CN103619466A (en) | 2014-03-05 |
PL2723490T3 (en) | 2021-03-08 |
US20120329930A1 (en) | 2012-12-27 |
EP2723490A4 (en) | 2015-01-28 |
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